Canonical Allele Identifier: CA3751679

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33189031C>G , CM000668.2:g.33189031C>G	GRCh38
NC_000006.11:g.33156808C>G , CM000668.1:g.33156808C>G	GRCh37
NC_000006.10:g.33264786C>G	NCBI36
NG_011589.1:g.8438G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682718.1:n.207G>C
ENST00000341947.7:c.390G>C MANE Select	ENSP00000339915.2:p.Arg130=
ENST00000341947.6:c.390G>C	ENSP00000339915.2:p.Arg130=
ENST00000361917.5:c.390G>C	ENSP00000355123.1:p.Arg130=
ENST00000374708.8:c.390G>C	ENSP00000363840.4:p.Arg130=
ENST00000395194.1:c.390G>C	ENSP00000378620.1:p.Arg130=
ENST00000457788.5:c.390G>C	ENSP00000405520.1:p.Arg130=
NM_001163771.1:c.390G>C	NP_001157243.1:p.Arg130=
NM_080679.2:c.390G>C	NP_542410.2:p.Arg130=
NM_080680.2:c.390G>C	NP_542411.2:p.Arg130=
NM_080681.2:c.390G>C	NP_542412.2:p.Arg130=
XM_011514298.1:c.-457G>C	XP_011512600.1:n.-457G>C
XM_017010250.1:c.390G>C	XP_016865739.1:p.Arg130=
NM_001163771.2:c.390G>C	NP_001157243.1:p.Arg130=
NM_080680.3:c.390G>C MANE Select	NP_542411.2:p.Arg130=
NM_080681.3:c.390G>C	NP_542412.2:p.Arg130=
NM_080679.3:c.390G>C	NP_542410.2:p.Arg130=